Journal
NATURE REVIEWS DISEASE PRIMERS
Volume 8, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41572-022-00365-7
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Funding
- Deutsche Forschungsgemeinschaft (DFG) [KU 1587/6-1, SE 1839/2-1]
- Austrian Science Fund (FWF)
- Swiss National Science Foundation (SNSF)
- Scientific and Technological Research Council of Turkey (TUBITAK)
- European Union [825575]
- Interdisciplinary Centre for Clinical Research within the faculty of Medicine at the RWTH Aachen University [IZKF TN1-1/IA 532001, IZKF TN1-2/IA 532002]
- Medical Research Council [MR/R011737/1]
- Wellcome Trust
- Versus Arthritis [21950]
- NIHR Cambridge Biomedical Research Centre [BRC-1215-20014]
- Association Belge contre les Maladies Neuromusculaires (ABMM)
- Research Fund -Flanders (FWO) [1805021N]
- DOC-PR04 PhD fellowship from the University of Antwerp
- Solve-RD EU [779257]
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This article discusses the epidemiology, pathophysiology, diagnosis and treatment of genetic pain loss disorders, which are characterized by reduced pain sensation. The development of these disorders is associated with recurrent injuries, burns and poorly healing wounds. Current treatment options mainly focus on symptomatic relief, but targeted therapies are being explored. The understanding of the genes and mechanisms related to pain loss disorders also provides new insights for the development of innovative pain medicines.
Genetic pain loss disorders are a heterogeneous group of diseases that are characterized by reduced pain sensation. This Primer discusses the epidemiology, pathophysiology, diagnosis and treatment of these disorders. Genetic pain loss includes congenital insensitivity to pain (CIP), hereditary sensory neuropathies and, if autonomic nerves are involved, hereditary sensory and autonomic neuropathy (HSAN). This heterogeneous group of disorders highlights the essential role of nociception in protecting against tissue damage. Patients with genetic pain loss have recurrent injuries, burns and poorly healing wounds as disease hallmarks. CIP and HSAN are caused by pathogenic genetic variants in >20 genes that lead to developmental defects, neurodegeneration or altered neuronal excitability of peripheral damage-sensing neurons. These genetic variants lead to hyperactivity of sodium channels, disturbed haem metabolism, altered clathrin-mediated transport and impaired gene regulatory mechanisms affecting epigenetic marks, long non-coding RNAs and repetitive elements. Therapies for pain loss disorders are mainly symptomatic but the first targeted therapies are being tested. Conversely, chronic pain remains one of the greatest unresolved medical challenges, and the genes and mechanisms associated with pain loss offer new targets for analgesics. Given the progress that has been made, the coming years are promising both in terms of targeted treatments for pain loss disorders and the development of innovative pain medicines based on knowledge of these genetic diseases.
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